Canonical Allele Identifier: PA161972
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 135189
ClinVar RCV Id: RCV000121996 RCV000409013 RCV000461515 RCV000570658 RCV000410596 RCV000758696 RCV001650985
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Glu480Lys
CA007585
NM_020630.6:c.1438G>A